Dlp Select 3d Arterial Cannula And Dlp Elongated One Piece Arterial Cannulae

Recall Summary DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae are being recalled across Canada due to sterility concerns. These are medical devices used during cardiac surgery procedures. The recall is classified as Class II, meaning the devices may not meet required sterility standards.

Product

DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae

Reason

Performance - Sterility

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-07-03

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b8ad056a-60ef-4b95-a695-2a07b12157ba